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[ CAS No. 72411-52-0 ]

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3d Animation Molecule Structure of 72411-52-0
Chemical Structure| 72411-52-0
Chemical Structure| 72411-52-0
Structure of 72411-52-0 * Storage: {[proInfo.prStorage]}
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Product Details of [ 72411-52-0 ]

CAS No. :72411-52-0 MDL No. :MFCD10565813
Formula : C9H8FN3 Boiling Point : -
Linear Structure Formula :- InChI Key :QYEHDCXFXONDPV-UHFFFAOYSA-N
M.W :177.18 Pubchem ID :2759138
Synonyms :

Safety of [ 72411-52-0 ]

Signal Word:Danger Class:8
Precautionary Statements:P261-P280-P305+P351+P338 UN#:3259
Hazard Statements:H302-H315-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 72411-52-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 72411-52-0 ]

[ 72411-52-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4640-67-9 ]
  • [ 72411-52-0 ]
YieldReaction ConditionsOperation in experiment
96% With hydrazine hydrate; In methanol; at 150℃; for 0.0833333h;Microwave irradiation; General procedure: A microwave tube was charged with ketonitrile (2.0 mmol), methanol (1 mL), and hydrazine monohydrate (2.6 mmol) and subjected to microwave irradiation (100 W, 150 C) for 5 minutes. Volatiles were subsequently removed under reduced pressure. The residue was purified by either trituration with cold methanol or cyclohexane, or by using column chromatography to give the final product.
  • 2
  • [ 4640-67-9 ]
  • [ 129117-13-1 ]
  • [ 72411-52-0 ]
YieldReaction ConditionsOperation in experiment
With hydrazine hydrate; In ethanol; for 3h;Reflux; A solution of <strong>[4640-67-9]3-(4-fluorophenyl)-3-oxopropanenitrile</strong> (470 mg, 60 % purity, 1.73 mmol, CAS 4640-67-9) in ethanol (3.6 mL) was treated with hydrazine hydrate (1 :1) (100 mu, 2.1 mmol). The mixture was refluxed for 3 h and stirred over the weekend at room temperature. The mixture was diluted with started sodium hydrogen carbonate solution, ethanol was removed under reduced pressure. The resulting precipitate was collected by filtration. The filtrate was also taken to dryness and combined with the precipitate to yield 360 mg of a approx. 2: 1 mixture of 3-(4-fluorophenyl)-1H-pyrazol-5-amine together with 3-(4-ethoxyphenyl)-1H-pyrazol-5-amine. The mixture was used in the next reaction. LC-MS (method 10): Rt = 0.87 min; MS (ESIpos): m/z = 178 [M+H]+ / Rt = 0.97 min; MS (ESIpos): m/z = 204 [M+H]+
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